Join NDA and get the chance to work with some of the leading minds in regulatory affairs, pharmacovigilance, health technology assessment and scientific communications on a variety of projects, clients and geographies.
What do we do?
NDA leads the field in providing regulatory drug and device development advice to the global life science industry as well as managing critical agency interactions and milestone meetings, such as FDA Advisory Committee Meetings and CHMP Oral Explanations.
We have over 150 dedicated consultants employed and continue to grow across Europe and the USA. Our staff includes industry experts and many ex-regulators, assisted by an excellent support team, all with a passion and drive to help clients get good medicines to patients in need.
Expanding Client Base
Over the years NDA has supported over 1 000 individual life science companies and work on a steady basis with over 400 different companies ranging from global large pharma to niche startups. Our work spans a variety of different projects and therapeutic areas and we interact across all levels of our clients’ organisations.
As an organisation we have exciting expansion plans globally and anyone joining NDA will become an integral part of that journey. Today our offices are located in Sweden, Germany, USA, Switzerland, France and the United Kingdom, and our network spans across all of Europe and the US.
Privacy Notice For Candidates
As part of any recruitment activity, we collect and process Job Applicants’ personal data. At NDA we are committed to being transparent about how we collect and use your data whilst we meet our data protection obligations. Please read our Privacy Notice for Candidates for more information on how we handle your data.
Your drug development needs are unique
Contact us to learn how our experts can support you to meet all regulatory, quality and safety requirements and ensure the best path to approval.
Let's Bring Medicines to the World